Sodium borohydride → HCID 178476301, Verbindung

HRID 1486217

Reaktionsgleichung

Reaktionsgleichung von HRID 1486217
C(O)CO.C(=O)=O.[C:8]([O:11][CH2:12][CH2:13][C@H:14]1[CH2:19][CH2:18][C@H:17]([CH:20]([NH:24][C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:21][CH:22]=[O:23])[CH2:16][CH2:15]1)(=[O:10])[CH3:9].[BH4-].[Na+]>C(O)C>[C:8]([O:11][CH2:12][CH2:13][C@H:14]1[CH2:19][CH2:18][C@H:17]([CH:20]([NH:24][C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:21][CH2:22][OH:23])[CH2:16][CH2:15]1)(=[O:10])[CH3:9]

Komponenten

5

Edukt 3

HCID 4311764Sodium borohydrideHCID 86601574Dry ice ethyleneglycolHCID 178476300HCID 178476300, Verbindung

Produkt 1

HCID 178476301HCID 178476301, VerbindungAusbeute 53 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a cooled (ethylene glycol+dry ice) solution of 2-(trans-4-(1-(tert-butoxycarbonylamino)-3-oxopropyl)cyclohexyl)ethyl acetate (1.88 g, 5.5 mmol) in ethanol (90 mL) was added NaBH4 (0.212 g, 5.5 mmol). The mixture was stirred at −10˜15° C. for 10 min and 0° C. for 10 min, and then quenched by addition of saturated aqueous NH4Cl solution (30 mL) and brine (30 mL). After removal of the volatile by evaporation, the aqueous residue was extracted with EtOAc, dried over Na2SO4. Purification by flash column chromatography (eluent: 30% EtOAc in hexanes to 40%) gave the alcohol product (1.0 g, 53%). LC/MC: 366.1 (MNa)+.

Aufarbeitung

  1. customquenched by addition of saturated aqueous NH4Cl solution (30 mL) and brine (30 mL)
  2. customAfter removal of the
  3. customvolatile by evaporation
  4. extractionthe aqueous residue was extracted with EtOAc
  5. dry with materialdried over Na2SO4
  6. customPurification by flash column chromatography (eluent: 30% EtOAc in hexanes to 40%)

Quellen und Nachweise

ORD-Eintrag
ord-a1d9572169cb42218c691f0f2f162e02
Quelldatensatz
uspto-grants-2016_08
Patentnummer
US09422314B2

Verknüpfte Notizen

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